Homotopic functional connectivity disruptions in schizophrenia and their associated gene expression

IF 4.7 2区 医学 Q1 NEUROIMAGING NeuroImage Pub Date : 2024-02-20 DOI:10.1016/j.neuroimage.2024.120551
Mengjing Cai , Yuan Ji , Qiyu Zhao , Hui Xue , Zuhao Sun , He Wang , Yijing Zhang , Yayuan Chen , Yao Zhao , Yujie Zhang , Minghuan Lei , Chunyang Wang , Chuanjun Zhuo , Nana Liu , Huaigui Liu , Feng Liu
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Abstract

It has been revealed that abnormal voxel-mirrored homotopic connectivity (VMHC) is present in patients with schizophrenia, yet there are inconsistencies in the relevant findings. Moreover, little is known about their association with brain gene expression profiles. In this study, transcription-neuroimaging association analyses using gene expression data from Allen Human Brain Atlas and case-control VMHC differences from both the discovery (meta-analysis, including 9 studies with a total of 386 patients and 357 controls) and replication (separate group-level comparisons within two datasets, including a total of 258 patients and 287 controls) phases were performed to identify genes associated with VMHC alterations. Enrichment analyses were conducted to characterize the biological functions and specific expression of identified genes, and Neurosynth decoding analysis was performed to examine the correlation between cognitive-related processes and VMHC alterations in schizophrenia. In the discovery and replication phases, patients with schizophrenia exhibited consistent VMHC changes compared to controls, which were correlated with a series of cognitive-related processes; meta-regression analysis revealed that illness duration was negatively correlated with VMHC abnormalities in the cerebellum and postcentral/precentral gyrus. The abnormal VMHC patterns were stably correlated with 1287 genes enriched for fundamental biological processes like regulation of cell communication, nervous system development, and cell communication. In addition, these genes were overexpressed in astrocytes and immune cells, enriched in extensive cortical regions and wide developmental time windows. The present findings may contribute to a more comprehensive understanding of the molecular mechanisms underlying VMHC alterations in patients with schizophrenia.

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精神分裂症的同位功能连接中断及其相关基因表达。
研究发现,精神分裂症患者体内存在异常的体素-镜像同位连接(VMHC),但相关研究结果并不一致。此外,人们对其与大脑基因表达谱的关联知之甚少。在这项研究中,研究人员利用艾伦人类脑图谱的基因表达数据和病例对照VMHC差异进行了转录-神经影像关联分析,包括发现阶段(荟萃分析,包括9项研究,共386名患者和357名对照)和复制阶段(两个数据集内单独的组水平比较,共包括258名患者和287名对照),以确定与VMHC改变相关的基因。研究人员还进行了富集分析,以确定已识别基因的生物功能和特定表达,并进行了Neurosynth解码分析,以研究精神分裂症患者认知相关过程与VMHC改变之间的相关性。在发现和复制阶段,与对照组相比,精神分裂症患者表现出一致的VMHC变化,这些变化与一系列认知相关过程相关;元回归分析表明,病程与小脑和中央后回/中央前回的VMHC异常呈负相关。VMHC异常模式与1 287个富含基本生物过程(如细胞通讯调控、神经系统发育和细胞通讯)的基因稳定相关。此外,这些基因在星形胶质细胞和免疫细胞中过度表达,富集于广泛的皮质区域和宽泛的发育时间窗口。本研究结果有助于更全面地了解精神分裂症患者体内 VMHC 改变的分子机制。
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来源期刊
NeuroImage
NeuroImage 医学-核医学
CiteScore
11.30
自引率
10.50%
发文量
809
审稿时长
63 days
期刊介绍: NeuroImage, a Journal of Brain Function provides a vehicle for communicating important advances in acquiring, analyzing, and modelling neuroimaging data and in applying these techniques to the study of structure-function and brain-behavior relationships. Though the emphasis is on the macroscopic level of human brain organization, meso-and microscopic neuroimaging across all species will be considered if informative for understanding the aforementioned relationships.
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